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Neulasta

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pegfilgrastim

Neulasta

Pharmacologic class: Granulocytic colony stimulating factor

Action

Binds to specific cell-surface receptors on hematopoietic cells, stimulating their proliferation and differentiation in bone marrow

Availability

Injection: 6 mg/0.6 ml in prefilled syringes

Indications and dosages

To reduce risk of infection in non-myeloid cancer patients who are receiving myelosuppressive drugs

Adults: 6 mg subcutaneously as a single dose once per chemotherapy cycle

Contraindications

• Hypersensitivity to drug, Escherichia coli-derived proteins, filgrastim, or other drug components

Precautions

Use cautiously in:

• myeloid cancers, sickle cell disease

• patients undergoing chemotherapy or radiation

• pregnant or breastfeeding patients

• children (safety and efficacy not established).

Administration

• Inspect solution for particles; discard if particles or discoloration appear.

• Don't give 14 days before to 24 hours after administration of cytotoxic chemotherapy.

Adverse reactions

CNS: headache, weakness, fatigue, dizziness, insomnia

CV: peripheral edema

GI: nausea, vomiting, diarrhea, abdominal pain, dyspepsia, stomatitis, splenic rupture

Hematologic: leukocytosis, granulo-cytopenia

Musculoskeletal: bone pain, myalgia, joint pain

Respiratory: adult respiratory distress syndrome (ARDS) in septic patients

Skin: alopecia, mucositis

Other: taste perversion, allergic reaction, increased pain, fever, neutropenic fever, aggravation of sickle cell disease

Interactions

Drug-drug. Lithium: potentiation of neutrophil release

Drug-diagnostic tests. Alkaline phosphatase, lactate dehydrogenase, uric acid: increased levels

Patient monitoring

Assess for signs and symptoms of impending splenic rupture, such as left upper abdominal quadrant or shoulder pain and splenic enlargement.

• Monitor vital signs and temperature.

Watch for signs and symptoms of sepsis, ARDS, and neutropenic fever.

• Monitor CBC, uric acid level, and liver function tests.

Patient teaching

• Teach patient or caregiver how to administer injection and dispose of syringes at home, if appropriate.

Teach patient to recognize and immediately report respiratory distress or signs and symptoms of splenic rupture.

• Caution patient to avoid driving and other hazardous activities until he knows how drug affects concentration and alertness.

• Advise patient to minimize GI upset by eating small, frequent servings of food and drinking plenty of fluids.

• Instruct patient to have follow-up laboratory tests as needed.

• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs and tests mentioned above.

McGraw-Hill Nurse's Drug Handbook, 7th Ed. Copyright © 2013 by The McGraw-Hill Companies, Inc. All rights reserved

Neulasta

A brand name for PEGFILGASTRIM.
Collins Dictionary of Medicine © Robert M. Youngson 2004, 2005
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References in periodicals archive
As such, it is indicated in the exact same way as subcutaneous (pre-filled syringe) Neulasta.
A comprehensive analytical, biofunctional, preclinical and clinical comparability programme has demonstrated a high degree of similarity between Pelmeg and Neulasta. The Pelmeg confirmed biosimilarity to Neulasta in sensitive clinical study settings, demonstrated pharmacokinetic comparability to Neulasta at the clinical dose of 6 mg as well as pharmacodynamic comparability to Neulasta at the clinical dose of 6 mg and at the reduced dose of 3 mg, added the network.
--Generic (Biosimilar) Neulasta launches on schedule; generic Advair is delayed but launches by 2019.
The announcement sees the Mundipharma network (including NAPP Pharmaceuticals in the UK) gain immediate access to Pelmeg (B12019), a biosimilar to Neulasta (pegfilgrastim), which received CHMP recommendation for approval on 20 September 2018.
TUESDAY, June 5, 2018 (HealthDay News) -- The first biosimilar drug to Neulasta has been approved by the U.S.
The 50-50joint venture was launched in 1984 to fund the global development of Epogen (epoetin alfa) and, over time, was expanded to include Neupogen (filgrastim), Neulasta (pegfilgrastim), Aranesp (darbepoetin alfa), Nplate (romiplostim) and brodalumab.
For instance, many patients receiving chemotherapy receive a Neulasta shot after chemo to help keep the white counts from plummeting.
Neupogen (filgrastim) and Neulasta (prefilgrastim) are used to treat neutropenia, which promotes leukocytopoiesis; they were developed by Memorial Sloan Kettering Cancer Center (MSK) from 1970 and are FDA approved and sold by Amgen.
Its products include Prolia for osteoporosis, Enbrel for rheumatoid arthritis and skin disorders, and Neulasta and Neupogen for fighting infection in cancer patients.
Neupogen and Neulasta, two products that stimulate production of white blood cells had sales of $4.84 billion in 2010.
Neulasta and NEUPOGEN sales increased 12 percent to $1,021 million in the fourth quarter of 2011 versus $914 million in the fourth quarter of 2010, primarily driven by an increase in the average net sales price, and to a lesser extent, favorable changes in wholesaler inventories.
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